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Cerebellar Regional Dissection for Molecular Analysis
Published on: December 5, 2020
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Cerebellar restricted diffusion in Wernicke's encephalopathy.
Narenraj Arulprakash1, Vishank Shah2
1Department of Neurology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, United States.
Journal of Neurosciences in Rural Practice
|March 9, 2023
Summary
This case highlights Wernicke's encephalopathy, a neurological condition caused by thiamine deficiency, presenting with severe symptoms after medical procedures. Prompt thiamine replacement led to partial neurological recovery and imaging improvements.
Area of Science:
- Neurology
- Internal Medicine
- Radiology
Background:
- A 50-year-old woman with a history of uterine cancer and chronic radiation enteritis presented with acute lower limb pain, later diagnosed with aortoiliac stenosis.
- Following stent placement, she developed altered mental status, ataxia, and ophthalmoplegia, rapidly progressing to a stuporous state.
Purpose of the Study:
- To report a complex case of Wernicke's encephalopathy presenting atypically in a patient with risk factors including poor oral intake and prior chemoradiation.
- To correlate clinical presentation with neuroimaging findings suggestive of thiamine deficiency.
- To emphasize the importance of considering Wernicke's encephalopathy despite potentially normal or falsely elevated thiamine levels.
Main Methods:
- Clinical case presentation with detailed neurological examination and patient history.
- Neuroimaging including Magnetic Resonance Imaging (MRI) of the brain, focusing on diffusion-weighted imaging (DWI) and T2-FLAIR sequences.
- Biochemical testing of serum thiamine levels and consideration of factors affecting assay results (enteral feeds).
- Therapeutic intervention with high-dose intravenous thiamine replacement.
Main Results:
- MRI revealed restricted diffusion and T2-FLAIR hyperintensities in the cerebellum, dorsomedial thalami, and fornix, with mammillary body enhancement, consistent with Wernicke's encephalopathy.
- Serum thiamine level was borderline (70 nmol/l), potentially falsely elevated due to enteral feeding.
- Following thiamine treatment, repeat MRI showed resolution of acute changes with mild cerebellar atrophy, and the patient exhibited subtle neurological improvement.
Conclusions:
- Wernicke's encephalopathy can present with diverse neurological deficits and imaging findings, sometimes masked by other medical conditions or laboratory results.
- Early recognition and aggressive thiamine repletion are crucial for improving outcomes in patients with suspected Wernicke's encephalopathy, even with non-specific or borderline thiamine levels.
- This case underscores the importance of a high index of suspicion for thiamine deficiency in patients with altered mental status and neurological deficits, particularly those with risk factors such as malnutrition or gastrointestinal issues.
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